Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.65077597A>G , CM000677.2:g.65077597A>G | GRCh38 |
| NC_000015.9:g.65369935A>G , CM000677.1:g.65369935A>G | GRCh37 |
| NC_000015.8:g.63156988A>G | NCBI36 |
| NG_021411.1:g.5782A>G , LRG_682:g.5782A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432196.5:c.782A>G MANE Select | ENSP00000388723.2:p.Tyr261Cys | |
| ENST00000432196.3:c.782A>G | ENSP00000388723.2:p.Tyr261Cys | |
| NM_001101362.2:c.782A>G , LRG_682t1:c.782A>G | NP_001094832.1:p.Tyr261Cys | |
| NM_001101362.3:c.782A>G MANE Select | NP_001094832.1:p.Tyr261Cys |